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Biocatalytic Polyester Synthesis in Supercritical Carbon Dioxide, Ionic Liquids and Organic Solvents

机译:超临界二氧化碳,离子液体和有机溶剂中生物催化聚酯的合成

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摘要

The use of enzymes as catalysts in chemical reactions has been an intense area of research for many years. Biocatalysis allows for reactions which would normally require high temperatures and pressures, as well as corrosive acid catalysts, to be carried out at ambient conditions while being highly selective. By pairing enzymes with environmentally benign solvents, such as supercritical carbon dioxide and ionic liquids, the detrimental impact of traditional chemical processes on the environment could be significantly reduced.Polyester synthesis in supercritical carbon dioxide would allow for the rational control of polymer molecular weight and dispersity due to the solvent tunability of supercritical fluids. In order to overcome poor monomer solubility in carbon dioxide, fluorinated monomers were substituted. Thus, fluorinated polyester synthesis was performed from activated diesters and fluorinated diols and the factors that would limit chain extension were assessed. Weight average molecular weights of up to 8094 Da were achieved. The phase behavior of each monomer, as well as the polyester product, was also studied. Additionally, hydroxylated monomers were incorporated into the synthesis in order to produce polyesters that had fluorinated, hydrogenated, and hydroxylated segments.In the Novozym® 435-catalyzed reaction between divinyl adipate and 1,4-butanediol, carbon dioxide was also employed as a viscosity reducing agent in order to alleviate some of the mass transfer limitations that occur during the polymerization. The presence of CO2 did enhance polymer molecular weight but only at reaction times of 1 hour or less. At reaction times longer than 1 hour, the presence of CO2 hindered the achievable molecular weight. Ionic liquids are another environmentally friendly solvent in which enzymatic reactions can be carried out. The enzymes Novozym® 435 and porcine pancreatic lipase were found to show enhanced stability in an ionic liquid when compared to a traditional organic solvent. The biocatalytic polymerization between divinyl adipate and 1,4-butanediol was carried out in this medium but polymer molecular weight was limited due to the precipitation of the polymer from the ionic liquid.
机译:多年来,在化学反应中使用酶作为催化剂一直是研究的重点领域。生物催化使通常需要高温和高压的反应以及腐蚀性酸催化剂可以在环境条件下进行,同时具有很高的选择性。通过将酶与环境友好的溶剂(例如超临界二氧化碳和离子液体)配对使用,可以显着降低传统化学工艺对环境的不利影响。超临界二氧化碳中的聚酯合成可以合理控制聚合物的分子量和分散性由于超临界流体的溶剂可调性。为了克服差的单体在二氧化碳中的溶解度,氟化单体被取代。因此,由活化的二酯和氟化的二醇进行了氟化聚酯的合成,并评估了限制链增长的因素。重均分子量达到了8094 Da。还研究了每种单体以及聚酯产品的相行为。此外,将羟基化的单体引入合成中以生产具有氟化,氢化和羟基化链段的聚酯。在Novozym®435催化的己二酸二乙烯基酯和1,4-丁二醇之间的反应中,还使用二氧化碳作为粘度还原剂以减轻聚合过程中发生的某些传质限制。 CO 2的存在确实提高了聚合物的分子量,但仅在1小时或更短的反应时间就提高了。在超过1小时的反应时间下,CO2的存在阻碍了可达到的分子量。离子液体是可以在其中进行酶促反应的另一种环境友好型溶剂。与传统的有机溶剂相比,发现Novozym®435酶和猪胰脂肪酶在离子液体中显示出增强的稳定性。在该介质中进行了己二酸二乙烯酯和1,4-丁二醇之间的生物催化聚合反应,但是由于聚合物从离子液体中沉淀出来,聚合物分子量受到限制。

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    Jesionowski Anita Mesiano;

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  • 年度 2002
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  • 原文格式 PDF
  • 正文语种 en
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